EBM Clinical Research Services
EBM Clinical Research Services Ltd. is a provider of clinical research services with a focus on conducting Phase II to Phase IV studies. Established by a highly skilled clinical research team with global experience and local expertise, the company aims to bridge international clients with local clinical research staff. It is registered with the Turkish Ministry of Health and is located in Istanbul, Turkey. The company values scientific excellence, integrity, and a commitment to helping develop and deliver medicines and healthcare products to help patients.
Industries
Nr. of Employees
small (1-50)
EBM Clinical Research Services
Products
Outsource CRO Clinical Research Organization
EBM provides outsource clinical research services supporting pharmaceutical, biotechnology, and medical device companies across the full clinical trial lifecycle, combining international standards with local expertise.
Outsource CRO Clinical Research Organization
EBM provides outsource clinical research services supporting pharmaceutical, biotechnology, and medical device companies across the full clinical trial lifecycle, combining international standards with local expertise.
Services
Operational conduct of interventional and observational clinical studies across Phase I–IV, including protocol support and study execution.
Feasibility evaluations to assess site suitability, patient availability and operational readiness.
Preparation and submission of study documents to ethics committees and national regulatory authorities.
Assistance with import licensing and customs clearance processes required for investigational products and devices.
Site qualification, initiation, monitoring and closure visits to ensure protocol adherence and data integrity.
Support for study design, endpoint definition and protocol drafting.
Operational conduct of interventional and observational clinical studies across Phase I–IV, including protocol support and study execution.
Feasibility evaluations to assess site suitability, patient availability and operational readiness.
Preparation and submission of study documents to ethics committees and national regulatory authorities.
Assistance with import licensing and customs clearance processes required for investigational products and devices.
Site qualification, initiation, monitoring and closure visits to ensure protocol adherence and data integrity.
Support for study design, endpoint definition and protocol drafting.
Expertise Areas
- Clinical trial management (Phase II–IV and observational studies)
- Regulatory compliance and ethics submissions
- Clinical data management and biostatistics
- Medical writing and regulatory documentation
Key Technologies
- Clinical databases and data management systems
- Biostatistical analysis and reporting methods
- Electronic clinical data capture and study reporting tools
- Clinical trial management and site monitoring methodologies